Module 1: Introduction to Clinical Research

Module 2: Essential Clinical Trial Documents

Module 3: Evolution of Ethics, Regulations & Guidelines

Module 4: Informed Consent Process

Module 5: Institutional Review Board

Module 6: Overview of Cancer & Oncology Cancer Trials

Module 7: Diagnosing Cancer

Module 8: Safety Evaluation in Oncology Clinical Trials

Module 9: Efficacy Evaluation in Oncology Clinical Trials

Module 10: Development of Monitoring Plan

Module 11: Site Initiation, Documents Review & Delegation of Duties at Sites

Module 12: Clinical Trial Monitoring

Module 13: Inventory Planning and Tracking

Module 14: Source Document Verification (SDV)

Module 15: CRF Review & Data Management

Module 16: Safety Reporting & Regulatory Compliance

Module 17: IP Accountability & Management

Module 18: Escalation, Prevention & Management of Violation/Deviations

Module 19: Site Closure Visit